Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromo-2-methylaniline | HCID 11423 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phenylmalonic acid | HCID 75791 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Product | HCID 86716089 | HCID 86716089 | — |
Reaction Steps
A mixture of 2-phenylmalonic acid (7.62 g, 42.3 mmol) and POCl3 (32.8 mL, 352 mmol) was stirred at reflux (130° C. aluminum block temp) for 10 minutes, and the resulting homogeneous yellow solution was cooled on an ice bath. 4-Bromo-2-methylaniline (6.56 g, 35.2 mmol) was added in one portion and the mixture was refluxed for 2 hours. The dark solution was allowed to cool to room temperature and was diluted with DCM (70 mL) and ice (100 mL), and stirred under ambient conditions for ˜5-10 minutes at which point exothermic POCl3 hydrolysis commenced (ice bath cooling), and was then stirred at room temperature for another 30 minutes. The light yellow aqueous layer was extracted with DCM (1×30 mL), and the combined dark homogeneous organic layers were dried (Na2SO4), filtered, and concentrated with silica gel. The silica-adsorbed residue was dry load flash chromatographed with a 20% DCM/heptane to 100% DCM gradient to provide the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221804B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2ea90fbe06554ff2bf2cae64ba1cee97 |
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| Source note | uspto-grants-2015_12 |
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